Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Medigroup, Inc. with 15 510(k) clearances. The most recent is a 510(k) clearance dated May 21, 2012: FALLER TROCAR.
| Date | Record | Source |
|---|---|---|
| May 21, 2012 | FALLER TROCARK120130 · FJS | 510(k) clearances |
| Aug 31, 2007 | FLEX-NECK EXXTENDED PERITONEAL DIALYSIS CATHETER AND ACCESSORIES, MODEL CF-5560K071167 · FJS | 510(k) clearances |
| Jul 3, 2007 | FLEX-NECK ARC CATHETERK070730 · FJS | 510(k) clearances |
| Jul 18, 2006 | EMBEDDING TOOL, MODEL TE-1000K060897 · FJS | 510(k) clearances |
| Sep 17, 2003 | FLEX-NECK PD CATHETER, INFANTK031351 · FJS | 510(k) clearances |
| Feb 27, 1998 | PERITONEAL DIALYSIS CATHETER CONNECTORK974570 · FKO | 510(k) clearances |
| May 9, 1983 | MEDIGROUP LS-110 LIGHT SOURCEK823294 · HET | 510(k) clearances |
| May 6, 1983 | MEDIGROUP 2.2MM NEEDLESCOPE CANNULA&K823295 · HET | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
